ichthyosis–sclerosing cholangitis neonatal syndrome

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A rare autosomal recessive complex ichthyosis syndrome (ichthyosis with leucocyte vacuoles, alopecia, and sclerosing cholangitis) characterized by scalp hypotrichosis, scarring alopecia, vulgar type ichthyosis, and sclerosing cholangitis. It is caused by mutation in the gene for claudin-1.

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